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The Effectiveness of Associated Non-Pharmacological Measures in the prevention and redution the duration of Delirium subtypes in ICU patients

Not Applicable
Conditions
Delirium, transtornos neurocognitivos, delírios
F03.615
C10.597.606.337.500
Registration Number
RBR-6xq95s
Lead Sponsor
niversidade do Estado da Bahia
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Data analysis completed
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

Participants will be those over 18 years of age, with an expected length of stay in these units over 48 hours, who score in the E-PRE-DELIRIC score greater than or equal to 10% and who voluntarily agree to participate in the study

Exclusion Criteria

Patients who: are admitted to delirium; admitted to these ICUs, but who had had delirium in the previous hospitalization; are admitted in contact and / or respiratory precaution; receptive aphasia; Have severe hearing and / or visual disturbances that prevent adequate communication; To present psychiatric disorders, in acute phase, that cause cognitive alterations, like attention deficit and / or hallucinations; They are unable to understand Portuguese; Present scores on the Richmond Agitation-Sedation Scale (RASS) less than or equal to -3

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Occurrence of delirium in critically ill patients detected through the application of the flowsheet CAM-ICU scale. The delirium subtype will be identified from the score on the RASS scale
Secondary Outcome Measures
NameTimeMethod
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